1vry

Disease
Known disease associated with this structure: Hyperekplexia and spastic paraparesis OMIM:[138491], Startle disease, autosomal recessive OMIM:[138491], Startle disease/hyperekplexia, autosomal dominant OMIM:[138491]

About this Structure
1VRY is a 1 chain structure of sequence from Homo sapiens. This structure supersedes the now removed PDB entry 1zhd. Full experimental information is available from OCA.

Reference
Page seeded by OCA on Tue Feb 17 01:53:37 2009